Posts - Children's Liver Disease Foundation | HealthUnlocked

Children's Liver Disease Foundation

2,001 members • 703 posts

All posts for August 2012

3 year old son with Alpha 1

Hi my name is Cathy and my 3 year old son has always had problems with asthma and breathing since birth, he was finally referred to Hospital for tests as he...

Hi my name is Cathy and my 3 year old son has always had problems with asthma an...

benjollie

•12 years ago

6 Replies

York mum in limbo.

Hi Here I am introducing myself. My 12 year old son took ill in may this year. He had haematuria an enlarged spleen, portal hypertension ,...

Hi Here I am introducing myself. My 12 year old son took ill in may...

Yorkmum

•12 years ago

2 Replies

Hi I'm Diane and my eldest son Daniel was born with Biliary Atresia, had a Kasai at 7 wks but at 6 years old needed a Liver Transplant.

He has been very well since the transplant. Two years after transplant he was diagnosed as being Autistic. He starts Secondary school in September. He will...

He has been very well since the transplant. Two years after transplant he was di...

danielsmum

•12 years ago

4 Replies

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13 years later....

I want to introduce myself to all those on here. I am not a parent of a child with liver disease but an adult who was diagnosed with liver disease as a child....

I want to introduce myself to all those on here. I am not a parent of a child wi...

jenniwren

•12 years ago

9 Replies

Introduce yourself...

It's great to see so many of you have joined the community. Why not leave a short comment below and introduce yourselves. Give as much or as little...

It's great to see so many of you have joined the community. Why not leave a ...

Caitlin-CLDF

Partner•12 years ago

62 Replies

How did other people react to your child’s liver condition? Do you have any coping mechanisms or solutions to share?

Caitlin-CLDF

Partner•12 years ago

8 Replies

How did you feel when your child was diagnosed and how do you feel now?

Caitlin-CLDF

Partner•12 years ago

19 Replies

Welcome to CLDF's online community!

This is a place where you can talk to others, share your experiences and support one another through your journeys with childhood liver disease. Blogs are a...

This is a place where you can talk to others, share your experiences and support...

Caitlin-CLDF

Partner•12 years ago

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Posts - Children's Liver Disease Foundation | HealthUnlocked

Children's Liver Disease Foundation

All posts for August 2012

3 year old son with Alpha 1

York mum in limbo.

Hi I'm Diane and my eldest son Daniel was born with Biliary Atresia, had a Kasai at 7 wks but at 6 years old needed a Liver Transplant.

13 years later....

Introduce yourself...

How did other people react to your child’s liver condition? Do you have any coping mechanisms or solutions to share?

How did you feel when your child was diagnosed and how do you feel now?

Welcome to CLDF's online community!

Search posts

Pinned Posts

Latest poll

Where in the world are you from?

Topics

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